Famotidine

Product NDC
69842-063
11-digit product format
698420063
Labeler code
69842
Product ID
69842-063_b2736a1a-a748-45a8-8a9b-289f7dd61d14
Type
HUMAN OTC DRUG
Nonproprietary name
Famotidine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
CVS Pharmacy, Inc.
Application
ANDA206531
Marketing category
ANDA
Marketing start
2020-02-03
Substance
FAMOTIDINE
Active strength
10 mg/1
Pharmacologic classes
Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Famotidine
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FAMOTIDINE10 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii5QZO15J2Z8
Rxcui199047

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
396bde5c-c78e-2f8b-ab1f-2ee6ba32bcaeProduct name720260317
1e73f975-1ce7-705e-2bcf-788b1b5e24baProduct name520251124
cf645750-2e70-f6e1-c05a-a52847def5ddProduct name920250312
4fdc761c-585e-054b-8ebe-86130a26e4c1Product name220221205
fc2e1e31-353a-2c24-a4b4-fcf93bf7e38eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-063-19Famotidine90 in 1 BOTTLETABLET, FILM COATED909
69842-063-19Famotidine1 in 1 CARTONTABLET, FILM COATED19
69842-063-79Famotidine2 in 1 CARTONTABLET, FILM COATED29
69842-063-79Famotidine90 in 1 BOTTLETABLET, FILM COATED909
69842-063-84Famotidine30 in 1 BOTTLETABLET, FILM COATED309
69842-063-84Famotidine1 in 1 CARTONTABLET, FILM COATED19

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69842-063-19EA - Each69842-06354e478c6-7718-4b6c-bb56-9d7a79e6565f12023-06-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-063FAMOTIDINE TABLET, FILM COATED [CVS PHARMACY, INC.]9Current NDC, Legacy NDC, 6 package rows20250403_7357f67e-0fc6-4555-aa8b-1df09cba9feb.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
199047famotidine 10 MG Oral TabletPSN7357f67e-0fc6-4555-aa8b-1df09cba9feb9
199047famotidine 10 MG Oral TabletSCD7357f67e-0fc6-4555-aa8b-1df09cba9feb9

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69842-063-19698420063191 BOTTLE in 1 CARTON (69842-063-19) / 90 TABLET, FILM COATED in 1 BOTTLE1 bottle2020-02-030000-00-00NoNoCurrent
69842-063-79698420063792 BOTTLE in 1 CARTON (69842-063-79) / 90 TABLET, FILM COATED in 1 BOTTLE2 bottle2021-01-250000-00-00NoNoCurrent
69842-063-84698420063841 BOTTLE in 1 CARTON (69842-063-84) / 30 TABLET, FILM COATED in 1 BOTTLE1 bottle2020-02-030000-00-00NoNoCurrent